HSD17B4 purified MaxPab mouse polyclonal antibody (B01P)
产品名称： HSD17B4 purified MaxPab mouse polyclonal antibody (B01P)
英文名称： HSD17B4 purified MaxPab mouse polyclonal antibody (B01P)
产品编号： H00003295-B01P
产品价格： null
产品产地： 台湾
品牌商标： Abnova
更新时间： null
使用范围：
亚诺法生技股份有限公司（Abnova)
- 联系人 :
- 地址 : 台湾台北市内湖区洲子街 108 号 9 楼
- 邮编 : 11493
- 所在区域 : 台湾
- 电话 : +886-920**1152 点击查看
- 传真 : 点击查看
- 邮箱 : sales@abnova.com.tw
- Specification
- Product Description:
- Mouse polyclonal antibody raised against a full-length human HSD17B4 protein.
- Immunogen:
- HSD17B4 (ABM82792.1, 1 a.a. ~ 736 a.a) full-length human protein.
- Sequence:
- MGSPLRFDGRVVLVTGAGAGLGRAYALAFAERGALVVVNDLGGDFKGVGKGSLAADKVVEEIRRRGGKAVANYDSVEEGEKVVKTALDAFGRIDVVVNNAGILRDRSFARISDEDWDIIHRVHLRGSFQVTRAAWEHMKKQKYGRIIMTSSASGIYGNFGQANYSAAKLGLLGLANSLAIEGRKSNIHCNTIAPNAGSRMTQTVMPEDLVEALKPEYVAPLVLWLCHESCEENGGLFEVGAGWIGKLRWERTLGAIVRQKNHPMTPEAVKANWKKICDFENASKPQSIQESTGSIIEVLSKIDSEGGVSANHTSRATSTATSGFAGAIGQKLPPFSYAYTELEAIMYALGVGASIKDPKDLKFIYEGSSDFSCLPTFGVIIGQKSMMGGGLAEIPGLSINFAKVLHGEQYLELYKPLPRAGKLKCEAVVADVLDKGSGVVIIMDVYSYSEKELICHNQFSLFLVGSGGFGGKRTSDKVKVAVAIPNRPPDAVLTDTTSLNQAALYRLSGDWNPLHIDPNFASLAGFDKPILHGLCTFGFSARRVLQQFADNDVSRFKAIKARFAKPVYPGQTLQTEMWKEGNRIHFQTKVQETGDIVISNAYVDLAPTSGTSAKTPSEGGKLQSTFVFEEIGRRLKDIGPEVVKKVNAVFEWHITKGGNIGAKWTIDLKSGSGKVYQGPAKGAADTTIILSDEDFMEVVLGKLDPQKAFFSGRLKARGNIMLSQKLQMILKDYAKL
- Host:
- Mouse
- Reactivity:
- Human
- Storage Buffer:
- In 1x PBS, pH 7.2
- Storage Instruction:
- Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- Antibody reactive against mammalian transfected lysate.
- Application Image
- Western Blot (Transfected lysate)
- Detection Antibody
- Entrez GeneID:
- 3295
- GeneBank Accession#:
- DQ891866.2
- Protein Accession#:
- ABM82792.1
- Gene Name:
- HSD17B4
- Gene Alias:
- DBP,MFE-2,SDR8C1
- Gene Description:
- hydroxysteroid (17-beta) dehydrogenase 4
- Gene Ontology:
- Hyperlink
- Gene Summary:
- The protein encoded by this gene is a bifunctional enzyme that is involved in the peroxisomal beta-oxidation pathway for fatty acids. It also acts as a catalyst for the formation of 3-ketoacyl-CoA intermediates from both straight-chain and 2-methyl-branched-chain fatty acids. Defects in this gene that affect the peroxisomal fatty acid beta-oxidation activity are a cause of D-bifunctional protein deficiency (DBPD). An apparent pseudogene of this gene is present on chromosome 8. [provided by RefSeq
- Other Designations:
- 17-beta-HSD IV,17-beta-hydroxysteroid dehydrogenase 4,17beta-estradiol dehydrogenase type IV,3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholest-24-enoyl-CoA hydratase,D-3-hydroxyacyl-CoA dehydratase,D-bifunctional protein, peroxisomal,beta-hydroxyacyl deh
- Gene Pathway
- Related Disease
- Adenocarcinoma
- Asperger Syndrome
- Autistic Disorder
- Breast Neoplasms
- Cardiovascular Diseases
- Cryptorchidism
- Diabetes Mellitus, Type 2
- Edema
- Esophageal Neoplasms
- Genetic Predisposition to Disease
- Lung Neoplasms
- Neoplasms, Germ Cell and Embryonal
- Neoplasms, Glandular and Epithelial
- Neoplasms, Hormone-Dependent
- Obesity
- Ovarian cancer
- Ovarian Failure, Premature
- Ovarian Neoplasms
- Polycystic Ovary Syndrome